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Pioglitazon jako uzupełnienie terapii poznawczo-behawioralnej w zapobieganiu nawrotom uzależnienia od kokainy

4 września 2026 zaktualizowane przez: Joy Schmitz, The University of Texas Health Science Center, Houston

The purpose of this study is to see how well pioglitazone, when used with cognitive behavioral therapy, works at helping people who have recently stopped using cocaine to continue to not use cocaine.

Przegląd badań

Status

Zakończony

Warunki

Interwencja / Leczenie

Szczegółowy opis

Over one million American adults suffer from cocaine use disorder (CUD) with recent trends showing an increase in cocaine-related deaths since 2010. For the chronic cocaine user, significant changes in brain function and structure set the stage for relapse that, unfortunately, continues to be the most common outcome following treatment. For substance use disorders, cognitive-behavioral therapy (CBT) is arguably the most empirically supported and widely used relapse prevention approach. Considered to be a cognitive control therapy, CBT aims to improve 'top-down' executive control functions that are impaired in CUD and strongly connected to relapse. Converging evidence suggests that CBT promotes meaningful changes in brain regions associated with cognitive control. Still, many patients with cognitive impairments show suboptimal response to CBT, bolstering the call for research aimed at improving effects with integrative treatments.

The goal of this project is to enhance the relapse-prevention effects of CBT with adjunctive use of pioglitazone (PIO), a peroxisome proliferator-activated receptor gamma (PPAR-γ) agonist. Unlike traditional medications that target classic neurotransmitter systems, PIO's activation of the PPAR pathway confers broad spectrum anti-inflammatory and neuroprotective effects against insult to brain white matter (WM). The functional significance of WM in CUD has been well established by evidence showing that: (1) chronic cocaine exposure alters WM structural integrity; (2) WM alterations compromise cognitive function in CUD; and (2) better WM integrity predicts better CUD treatment outcome. In a recent proof of concept trial it was found that PIO significantly improved brain WM integrity in a small sample of non-abstinent patients with CUD. Treatment with PIO was well-tolerated and associated with reduced cocaine craving relative to placebo. Collectively, these findings raise the exciting possibility that PIO may augment responding to CBT via improved neural structure and cognitive function.

A randomized double-blind clinical trial will be utilized to evaluate the efficacy of CBT with adjunctive PIO in recently abstinent patients during the early phase of recovery when craving is prominent, relapse risk is high, and intact cognitive control is required to actively maintain abstinence. Upon completion of a 5-day inpatient detoxification, 60 adults with CUD will complete titration to full dose of randomized medication, either PIO (45mg daily) or placebo, and begin 12 weeks of outpatient CBT treatment while continuing to receive study medication. Specific aims will examine the effects of PIO on targeted mechanisms of change (WM integrity, cognitive function, cocaine craving) and demonstrate evidence linking clinical efficacy (abstinence, functional health) with mechanism engagement. Expected results will establish PIO as an adjunctive treatment that can be integrated with CBT to reduce relapse risk following detoxification, thereby meeting NIDA's strategic priority of evaluating the use of medications to improve the efficacy of behavioral interventions (PA-18-055).

Typ studiów

Interwencyjne

Zapisy (Rzeczywisty)

61

Faza

  • Faza 2

Kontakty i lokalizacje

Ta sekcja zawiera dane kontaktowe osób prowadzących badanie oraz informacje o tym, gdzie badanie jest przeprowadzane.

Lokalizacje studiów

  • Stany Zjednoczone
    • Texas
      • Houston, Texas, Stany Zjednoczone, 77054
        • UTHealth Center for Neurobehavioral Research on Addiction

Kryteria uczestnictwa

Badacze szukają osób, które pasują do określonego opisu, zwanego kryteriami kwalifikacyjnymi. Niektóre przykłady tych kryteriów to ogólny stan zdrowia danej osoby lub wcześniejsze leczenie.

Kryteria kwalifikacji

Wiek uprawniający do nauki

18 lat do 65 lat (Dorosły, Starszy dorosły)

Akceptuje zdrowych ochotników

Nie

Płeć kwalifikująca się do nauki

Wszystko

Opis

Inclusion Criteria:

  • 18 to 65 years old
  • meet DSM 5 diagnostic criteria for cocaine use disorder
  • report recent cocaine use, verified by at least one positive urine drug screen for the cocaine metabolite, benzoylecgonine, during intake
  • be judged by the medical staff to be psychiatrically stable and physically healthy
  • for females, be using an effective form of birth control (e.g., barrier, IUD, or sterilization) and not be pregnant as determined by a serum pregnancy test at screening and negative urine pregnancy test at intake prior to first dose of investigational drug (test will be repeated weekly to ensure that female patients do not continue in the study if pregnant) or lactating
  • be willing to be admitted to a 5-day inpatient detoxification program at The Right Step Houston
  • be able to understand the consent form and provide written informed consent
  • be able to provide the names of at least 2 persons who can consistently locate their whereabouts

Exclusion Criteria:

  • have an acute medical or psychiatric disorder that would, in the judgment of the study physician, make participation difficult or unsafe
  • have suicidal or homicidal ideation that requires immediate attention
  • have another current (≥ moderate) substance use disorder aside from alcohol, nicotine, or marijuana
  • have a medical condition contraindicating PIO pharmacotherapy (e.g., drug- or insulin-dependent diabetes, congestive heart failure, edema, clinical significant liver disease, hypoglycemia, history of bladder cancer) or be taking medications that would adversely interact with PIO (e.g., CYP2C8 inhibitors or inducers, antihyperglycemic medications)
  • be concurrently enrolled in other addiction treatment services aside from smoking cessation
  • if female, be currently pregnant, breastfeeding, or planning on conception
  • have conditions of probation or parole requiring reports of drug use to officers of the court
  • be unable to read, write, or speak English
  • be homeless (live on the street)
  • have medical contraindications to MRI/DTI scans (e.g., history of pacemaker, metal implants, or welding/metal work without protective eyewear)

Plan studiów

Ta sekcja zawiera szczegółowe informacje na temat planu badania, w tym sposób zaprojektowania badania i jego pomiary.

Jak projektuje się badanie?

Szczegóły projektu

  • Główny cel: Leczenie
  • Przydział: Randomizowane
  • Model interwencyjny: Przydział równoległy
  • Maskowanie: Poczwórny

Broń i interwencje

Grupa uczestników / Arm
Interwencja / Leczenie
Aktywny komparator: CBT + pioglitazone

Cognitive Behavioral Therapy will be administered twice weekly during weeks 1-4 and once weekly during weeks 5-12 and augmented with a pioglitazone (45 mg) capsule every day during weeks 1-12.
Behawioralne: Cognitive Behavioral Therapy (CBT)

All participants will receive evidence-based individual Cognitive Behavioral Therapy (CBT) shown to be an effective intervention for maintaining abstinence following detoxification. Trained masters-level licensed professional counselors will deliver CBT.

Inne nazwy:
  • CBT
Lek: Pioglitazone

Pioglitazone capsules will start at 30 mg (Detox days 3 and 4) and increase to fixed dose of 45 mg for study weeks 1-12 and will also contain riboflavin.

Inne nazwy:
  • Aktos
Komparator placebo: CBT + placebo

Cognitive Behavioral Therapy will be administered twice weekly during weeks 1-4 and once weekly during weeks 5-12 and augmented with a placebo capsule every day during weeks 1-12.
Behawioralne: Cognitive Behavioral Therapy (CBT)

All participants will receive evidence-based individual Cognitive Behavioral Therapy (CBT) shown to be an effective intervention for maintaining abstinence following detoxification. Trained masters-level licensed professional counselors will deliver CBT.

Inne nazwy:
  • CBT
Lek: Placebo

Placebo capsules will be filled with corn starch and riboflavin.

Inne nazwy:
  • Skrobia kukurydziana

Co mierzy badanie?

Podstawowe miary wyniku

Miara wyniku
Opis środka
Ramy czasowe
Change in white matter integrity as assessed by change in fractional anisotropy value measured by diffusion tensor imaging
Ramy czasowe: Week 0 and Week 12

Anisotropy values range from 0 to 1, where a higher value indicates greater white matter integrity.
Week 0 and Week 12
Change in white matter integrity as assessed by change in radial diffusivity value measured by diffusion tensor imaging
Ramy czasowe: Week 0 and Week 12

Radial diffusivity (RD) values are not bound by specified upper and lower ranges, as the metric is a derivation of two diffusion eigenvalues = ([lambda2 / lambda3] / 2). Higher RD values are indicative of decreased white matter integrity as related to myelin integrity; conversely lower RD scores indicate better white matter integrity.
Week 0 and Week 12
Change in working memory as assessed by the NIH Toolbox Cognition Battery List Sorting Task
Ramy czasowe: Week 0

The List Sorting Task has an age-adjusted scale score that ranges from 0 to 100, with a higher score indicating better performance.
Week 0
Change in working memory as assessed by the NIH Toolbox Cognition Battery List Sorting Task
Ramy czasowe: Week 4

The List Sorting Task has an age-adjusted scale score that ranges from 0 to 100, with a higher score indicating better performance.
Week 4
Change in working memory as assessed by the NIH Toolbox Cognition Battery List Sorting Task
Ramy czasowe: Week 12

The List Sorting Task has an age-adjusted scale score that ranges from 0 to 100, with a higher score indicating better performance.
Week 12
Change in attention/impulsivity as assessed by the NIH Toolbox Cognition Battery Flanker Test
Ramy czasowe: Week 0

The Flanker Test has an age-adjusted scale score that ranges from 0 to 100, with a higher score indicating better performance.
Week 0
Change in attention/impulsivity as assessed by the NIH Toolbox Cognition Battery Flanker Test
Ramy czasowe: Week 4

The Flanker Test has an age-adjusted scale score that ranges from 0 to 100, with a higher score indicating better performance.
Week 4
Change in attention/impulsivity as assessed by the NIH Toolbox Cognition Battery Flanker Test
Ramy czasowe: Week 12

The Flanker Test has an age-adjusted scale score that ranges from 0 to 100, with a higher score indicating better performance.
Week 12
Change in cognitive function as assessed by the NIH Toolbox Cognition Battery Fluid Cognition Composite score
Ramy czasowe: Week 0

The Fluid Cognition Composite score is the normed standardized score ranging from 0 to 145, with a higher score indicating better performance.
Week 0
Change in cognitive function as assessed by the NIH Toolbox Cognition Battery Fluid Cognition Composite score
Ramy czasowe: Week 4

The Fluid Cognition Composite score is the normed standardized score ranging from 0 to 145, with a higher score indicating better performance.
Week 4
Change in cognitive function as assessed by the NIH Toolbox Cognition Battery Fluid Cognition Composite score
Ramy czasowe: Week 12

The Fluid Cognition Composite score is the normed standardized score ranging from 0 to 145, with a higher score indicating better performance.
Week 12
Number of participants who don't relapse as assessed by continuous cocaine-negative urine drug screens in the final three weeks of treatment
Ramy czasowe: From Week 10 to Week 12

For a cocaine-negative urine drug screen result, benzoylecgonine levels must be under 150 ng/mL.
From Week 10 to Week 12
Self-reported craving for cocaine as assessed by average Brief Substance Craving Scale score across 12 weeks of treatment
Ramy czasowe: From Week 1 to Week 12

The Brief Substance Craving Scale (BSCS) score ranges from 0 to 4, with a higher score indicating greater craving. Participants will be assessed by BSCS once per week for 12 weeks, and the average BSCS score over the 12 weeks will be reported.
From Week 1 to Week 12
Self-reported craving for cocaine as assessed by average Visual Analogue Scale score across 12 weeks of treatment
Ramy czasowe: From Week 1 to Week 12

The Visual Analogue Scale (VAS) score ranges from 0 to 100, with a higher score indicating greater craving. Participants will be assessed by VAS once per week for 12 weeks, and the average VAS score over the 12 weeks will be reported.
From Week 1 to Week 12

Miary wyników drugorzędnych

Miara wyniku
Opis środka
Ramy czasowe
Total percentage of days abstinent during treatment as assessed by self-reported non-use days confirmed by cocaine-negative urine drug screen results
Ramy czasowe: From Week 1 to Week 12

For a cocaine-negative urine drug screen result, benzoylecgonine levels must be under 150 ng/mL.
From Week 1 to Week 12
Total percentage of cocaine-negative urine drug screens during treatment as assessed by number of cocaine-negative samples out of total number of urine samples provided
Ramy czasowe: From Week 1 to Week 12

For a cocaine-negative urine drug screen result, benzoylecgonine levels must be under 150 ng/mL.
From Week 1 to Week 12
Functional health status as assessed by the Patient-Reported Outcomes Measurement Information System (PROMIS) global health summary score
Ramy czasowe: Week 0

The PROMIS global health summary score is a T-score derived from the global physical health (GPH) and global mental health (GMH) items and ranges from 40 to 60, with a greater T-score indicating better functional health status.
Week 0
Functional health status as assessed by the Patient-Reported Outcomes Measurement Information System (PROMIS) global health summary score
Ramy czasowe: Week 4

The PROMIS global health summary score is a T-score derived from the global physical health (GPH) and global mental health (GMH) items and ranges from 40 to 60, with a greater T-score indicating better functional health status.
Week 4
Functional health status as assessed by the Patient-Reported Outcomes Measurement Information System (PROMIS) global health summary score
Ramy czasowe: Week 12

The PROMIS global health summary score is a T-score derived from the global physical health (GPH) and global mental health (GMH) items and ranges from 40 to 60, with a greater T-score indicating better functional health status.
Week 12

Współpracownicy i badacze

Tutaj znajdziesz osoby i organizacje zaangażowane w to badanie.

Sponsor

The University of Texas Health Science Center, Houston

Współpracownicy

National Institute on Drug Abuse (NIDA)

Śledczy

  • Główny śledczy: Joy M Schmitz, PhD, UT Houston
  • Główny śledczy: Scott D Lane, PhD, UT Houston

Daty zapisu na studia

Daty te śledzą postęp w przesyłaniu rekordów badań i podsumowań wyników do ClinicalTrials.gov. Zapisy badań i zgłoszone wyniki są przeglądane przez National Library of Medicine (NLM), aby upewnić się, że spełniają określone standardy kontroli jakości, zanim zostaną opublikowane na publicznej stronie internetowej.

Główne daty studiów

Rozpoczęcie studiów (Rzeczywisty)

23 sierpnia 2021

Zakończenie podstawowe (Rzeczywisty)

26 września 2025

Ukończenie studiów (Rzeczywisty)

15 października 2025

Daty rejestracji na studia

Pierwszy przesłany

8 kwietnia 2021

Pierwszy przesłany, który spełnia kryteria kontroli jakości

8 kwietnia 2021

Pierwszy wysłany (Rzeczywisty)

13 kwietnia 2021

Aktualizacje rekordów badań

Ostatnia wysłana aktualizacja (Rzeczywisty)

21 września 2026

Ostatnia przesłana aktualizacja, która spełniała kryteria kontroli jakości

4 września 2026

Ostatnia weryfikacja

1 września 2026

Więcej informacji

Terminy związane z tym badaniem

Słowa kluczowe

Dodatkowe istotne warunki MeSH

Inne numery identyfikacyjne badania

  • HSC-MS-19-0718
  • R01DA048026 (Grant/umowa NIH USA)

Plan dla danych uczestnika indywidualnego (IPD)

Planujesz udostępniać dane poszczególnych uczestników (IPD)?

NIE

Informacje o lekach i urządzeniach, dokumenty badawcze

Bada produkt leczniczy regulowany przez amerykańską FDA

Tak

Bada produkt urządzenia regulowany przez amerykańską FDA

Nie

produkt wyprodukowany i wyeksportowany z USA

Tak

Te informacje zostały pobrane bezpośrednio ze strony internetowej clinicaltrials.gov bez żadnych zmian. Jeśli chcesz zmienić, usunąć lub zaktualizować dane swojego badania, skontaktuj się z register@clinicaltrials.gov. Gdy tylko zmiana zostanie wprowadzona na stronie clinicaltrials.gov, zostanie ona automatycznie zaktualizowana również na naszej stronie internetowej .

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